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ArticleAIDS research and therapy2020

Possible role of plasma Galectin-9 levels as a surrogate marker of viremia in HIV infected patients on antiretroviral therapy in resource-limited settings.

Ashwini Shete, Sampada Dhayarkar, Ashwini Dhamanage, Smita Kulkarni, Manisha Ghate, Shashikala Sangle, Uttam Medhe, Vinita Verma, Shobini Rajan, Toshio Hattori and 1 more

Open access · goldAbstract read
In one paragraph

Article in AIDS research and therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.0field-weighted citation impact, top 25% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 19 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 6 institutions in 2 countries.

Ashwini SheteICMR-National AIDS Research Institute, 73-G Block, M.I.D.C, Bhosari, Pune, India. ashete@nariindia.org.ORCID 0000-0003-0791-2128
Sampada DhayarkarICMR-National AIDS Research Institute, 73-G Block, M.I.D.C, Bhosari, Pune, India.
Ashwini DhamanageICMR-National AIDS Research Institute, 73-G Block, M.I.D.C, Bhosari, Pune, India.
Smita KulkarniICMR-National AIDS Research Institute, 73-G Block, M.I.D.C, Bhosari, Pune, India.
Manisha GhateICMR-National AIDS Research Institute, 73-G Block, M.I.D.C, Bhosari, Pune, India.
Shashikala SangleB.J. Medical College and Sassoon General Hospital, Jai Prakash Narayan Road, Near Pune Railway Station, Pune, India.
Uttam MedheYashwantrao Chavan Memorial Hospital, Sant Tukaram Nagar, Pimpri, Pune, India.
Vinita VermaNational AIDS Control Organization, Chandralok Building, 36, Janpath, New Delhi, India.
Shobini RajanNational AIDS Control Organization, Chandralok Building, 36, Janpath, New Delhi, India.
Toshio HattoriKibi International University, Takahashi, Okayama, Japan.
Raman GangakhedkarICMR-National AIDS Research Institute, 73-G Block, M.I.D.C, Bhosari, Pune, India.
National AIDS Research Institute · INNational AIDS Control Organisation · INB. J. Medical College & Sassoon Hospital · INIndian Council of Medical Research · INKibi International University · JPNational Centre for Cell Science · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEarly detection of viremia in HIV infected patients on anti-retroviral therapy (ART) is important to prevent disease progression as well as accumulation of drug resistance mutations. This makes HIV viral load (VL) monitoring indispensable in HIV infected patients on ART. However VL, being an expensive test, results in heavy financial burden on health services. Hence, cheaper surrogate markers of viremia are desired to reduce overall cost of management of HIV infected patients.

methodsWe enrolled aviremic (n = 63, M:F = 31:32) and viremic (n = 43, M:F = 21:22) HIV infected patients at 1 year after ART initiation. Viremic individuals were identified as those having a plasma VL of more than 1000 copies/µl and aviremic individuals as less than 40 copies/µl. The study participants also included immuno-virologically discordant patients as they demonstrate differential degrees of immune-reconstitution and are likely to harbour concomitant infections influencing levels of immune-activation markers screened as the surrogate markers. Immune activation markers viz. plasma hs-CRP, soluble-CD14 and Galectin-9 levels were estimated by ELISA, IL-6 by luminex assay and percentages of CD38+ CD8+ cells were determined by flow cytometry. The levels were compared between viremic and aviremic patients and correlated with plasma viral load. Receiver operated curve (ROC) analysis was done for plasma Galectin-9 levels.

resultsViremic patients had significantly higher levels of Galectin-9 and %CD38+ CD8+ cells (p values < 0.0001) than aviremic patients. Levels of the other activation markers did not differ between viremic and aviremic individuals. Galectin-9 levels (r = 0.76) and %CD38+ CD8+ cells (r = 0.39) correlated positively with VL. Area under curve for Galectin-9 levels for distinguishing between viremic and aviremic individuals was 0.98. Youden index, sensitivity, specificity, positive predictive value and negative predictive value for Galectin-9 levels were 0.87, 0.97, 0.90, 0.87 and 0.98, respectively, at the cut-off value of 5.79 ng/ml.

conclusionsPlasma Galectin-9 levels could identify viremic individuals with sensitivity and specificity of more than 90%. Thus, they showed a potential to serve as a surrogate marker of viremia in HIV infected patients on ART and would have cost implications on HIV management especially in resource-limited settings. However, the findings need to be confirmed in the patients on ART for different durations of time.

Indexed as

AdultAnti-Retroviral AgentsAntiretroviral Therapy, Highly ActiveBiomarkersCross-Sectional StudiesFemaleGalectinsHealth ResourcesHIV InfectionsHumansMaleMiddle AgedViral LoadViremiaYoung AdultAnti-Retroviral AgentsBiomarkersGalectinsLGALS9 protein, humanGalectin-9HIVImmune-activation markersSurrogate markerViral load

Identifiers

PMID32678033
PMCPMC7364535
OpenAlexW3043142205

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.